Variant report

Variant rs390828
Chromosome Location chr6:167630896-167630897
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167624600-167632800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:167626200-167635000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr6:167626600-167631000 Weak transcription Placenta Amnion Placenta Amnion
4 chr6:167628200-167637200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr6:167628200-167638600 Weak transcription Fetal Brain Female brain
6 chr6:167629000-167632400 Enhancers Liver Liver
7 chr6:167629200-167632200 Weak transcription Fetal Brain Male brain
8 chr6:167630000-167635000 Weak transcription Fetal Intestine Small intestine
9 chr6:167630400-167632200 Weak transcription Fetal Intestine Large intestine
10 chr6:167630400-167633400 Enhancers HepG2 liver
11 chr6:167630400-167637200 Weak transcription Stomach Mucosa stomach

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